System and method for detection of rna species

ABSTRACT

The invention includes methods for determining the presence of a latent viral population by analyzing an RNA population from the virus with digital techniques, such as digital PCR or by sequencing cDNA produced from the RNA. The invention additional includes methods for determining the presence of latent viral populations by detecting and/or quantifying enzymes that are uniquely associated with the virus, e.g., reverse transcriptases.

RELATED APPLICATIONS

The present application claims the benefit of and claims priority to U.S. Provisional Application Ser. No. 61/922,307 filed Dec. 31, 2013; U.S. Provisional Application Ser. No. 62/001,963 filed May 22, 2014; and U.S. Provisional Application Ser. No. 62/036,419 filed Aug. 12, 2014, the content of each is incorporated by reference herein in its entirety.

FIELD OF THE INVENTION

The invention generally relates to droplet based amplification and methods for analyzing, detecting, and quantifying RNA including, but not limited to, miRNA and viral RNA.

BACKGROUND

Classical methods for detecting and quantifying RNA have proven challenging in many applications due to the characteristics of particular RNA species and/or the particular environment in which the RNA species exists. The methods for detection of small RNA species have included northern hybridization analysis and microarray analysis. However, it is generally appreciated that the sensitivity and selectivity of those methods is poor for detection of low-abundance small RNA species, and the workflow can be challenging and expensive. (What is generally referred to as “small RNA” comprises a genus of RNA molecules that include species of what are generally referred to as non-coding RNA. Examples of small RNA species include miRNA (micro RNA), piRNA (P-element induced wimpy testis interacting RNA), siRNA (small interfering RNA), ceRNA (competing endogenous RNA), saRNA (small activating RNA), etc.) For example, traditional approaches used for miRNA analysis include a step of cDNA synthesis using a reverse transcriptase enzyme (RNA-dependent DNA polymerase isolated from a retrovirus) and subsequent amplification from the cDNA, where the process consists of at least two sample processing steps requiring user intervention, carried out separately (e.g. what may be referred to as “2-step RT-PCR”). For example, in the first step, purified RNA molecules are converted to cDNA using target-specific primers (sometimes referred to as “RT primers”) or random hexamers, and reverse transcriptase enzyme. The cDNA products are then amplified and detected in a second qPCR or digital PCR step. Numerous attempts to convert the two-step method into a one-step method for measuring miRNAs have failed, primarily because they typically yield significant background noise that in many instances makes discrimination of true signals impossible. This is especially true when low amounts of the miRNA targets of interest are present in the sample, when multiplexing multiple miRNAs, or when multiplexing miRNA in combination with other targets.

As described above, one example of a small RNA species includes what is referred to as microRNA (miRNA), which is a short non-coding RNA that plays important roles in various physiological processes through the post-transcriptional regulation of gene expression. Species of miRNA generally function via base-pairing with complementary sequences within mRNA molecules causing translational repression or target degradation thus silencing the expression of the target gene. Typical mature miRNA species are about 22 nucleotides in length, and are differentially expressed in various cell and/or tissue types where an analysis of quantitative expression of miRNA species can be used to accurately identify a cell and/or tissue type. Species of miRNA are also found as stable molecules in peripheral body fluids accessible using non or minimally invasive methods (e.g. cerebral spinal fluid, blood, urine, etc.), where similar quantitative analysis can indicate the presence of cell and/or tissue types elsewhere in the system. For example miRNA may be found as cell free RNA or packaged into exosomal and microvesicluar compartments that can be analyzed from bodily fluids such as blood and/or serum.

Species of miRNA have been implicated in a number of diseases, such as cancer, diabetes, immune system diseases, muscle disorders, and neurological development and degeneration. For example, miRNA-21 is involved in several cancer types such as glioblastoma and astrocytoma, and miRNA deregulation has been found to be associated with some types of cancer. By measuring quantity of specific miRNA types, diseases can be identified and distinguished to aid in the determination of a treatment course.

Also, available methods for quantifying “latent” reservoirs of retrovirus in patients have been shown to be suboptimal where such quantification is important for effective evaluation of available therapeutic strategies to fully cure retroviral infections. Typically, retrovirus is a single stranded RNA virus capable of producing a DNA copy of itself that integrates into and is treated as part of the genome of the host cell (sometimes referred to as a “provirus”). This DNA copy may then remain dormant or “latent” for long periods of time until cues are received by the host cell and the provirus initiates the process of transcription-translation to produce active virus and its associated proteins (sometimes referred to as “replication-competent provirus”).

One particularly important example of retrovirus is human immunodeficiency virus (HIV). While antiretroviral therapies have greatly improved the lives of many infected with HIV, it is generally understood that HIV establishes latent infections in long-lived cells that form a reservoir of the virus even after years of treatment with highly active antiretroviral therapy (HAART). Actually curing HIV infection, thus, requires eliminating these long-lived reservoir cells. A typical reservoir of latent HIV resides in resting CD4+ memory T cells.

Because the latent population of cells represents an important metric in HIV health, researchers have long sought a method to quickly and precisely quantify the number of cells harboring latent provirus. However, the low frequency of these cells makes such an assay technical challenging. For example, for HIV-positive individuals on HAART, only about one in a million resting CD4 T cells contain latent proviruses capable of producing replication- competent virus. Accordingly, the low counts are often lost in the “noise” associated with biological assays. See, e.g., Eriksson et al., “Comparative Analysis of Measures of Viral Reservoirs in HIV-1 Eradication Studies,” PLOS, Pathogens, vol. 9 (2), e1003174, p. 1-17 (2013), incorporated herein by reference in its entirety.

The current gold-standard method of detecting latent HIV infection involves a limiting dilution viral outgrowth assay (also referred to as “VOA”) that is slow, resource-intensive, and relatively imprecise. The VOA assay also requires 120-160 ml of blood. Complicating matters further is the fact that defective HIV DNA is present at approximately 100- to 1000-fold excess over functional proviral HIV DNA resulting in overestimation of replication competent provirus, and underestimation can also occur due to replication competent provirus not being scored in the VOA.

Rapid, simple, accurate, and cost effective quantification methods for RNA species including small RNA and viral species are needed both to accelerate understanding of the role and biological function of these RNA species in normal and disease states, as well as for use in clinical diagnostics.

SUMMARY

Embodiments of the invention provide improved detection of RNA species that include small RNA, mRNA, and viral populations, such as latent retroviral populations, by isolating and quantifying RNA such as that associated with the latent virus or enzymes (e.g., reverse transcriptase) associated with the latent virus. Because the methods of the invention individually isolate each RNA (and/or enzyme) molecule in a fluidic droplet, it is possible to quickly quantify the amount of replication competent virus in a sample by simply counting the number of droplets meeting a criterion, or by determining the number of RNA or enzyme samples that have a viable sequence. Furthermore, because the isolated microenvironment facilitates superefficient reverse transcription, strand switching in the nucleic acid is minimized, resulting in sequence reads with higher fidelity, and greater confidence in the final results. For example, the methods are broadly applicable to determine RNA viral load, and the presence of enzymes associated with retroviruses. In some embodiments, the retrovirus is HIV.

The RNA detection process involves exposing the RNA to a primer and then synthesizing cDNA. The cDNA may optionally be amplified and quantified, or the cDNA may be directly sequenced. For example, the method may involve a one-step reverse transcription/amplification process. In some embodiments, the resulting cDNA will be labeled with a unique or semi- unique barcode that will facilitate identification of individual RNA molecules after sequencing. In some embodiments, a virion particle containing the RNA is isolated in an aqueous droplet, and the virion particle subsequently lysed to release the RNA. In other embodiments the virion particles may be lysed and then the RNA isolated into aqueous droplets. In some embodiments, the RNA sample is collected from highly purified resting CD4+ T cells.

In other embodiments, the detection process involves exposing the enzyme to a labeled probe with a specific binding for the enzyme. In some embodiments, the probe may include an antibody, i.e., a fluorescently-labeled antibody, or an ELISA-type probe. In other embodiments, enzymatic activity can be evaluated by encapsulating each enzyme with a known substrate (e.g. exogenous RNA) and the detecting the enzymatic products (e.g. qPCR type assay for the exogenous RNA that may include use of hydrolysis probes, or the use of a fluorogenic RNA substrate). In embodiments where the enzymes are quantified, the methods may involve collecting enzymes from a lysate of a cell population containing the latent virus.

Using the methods of the invention, it is straightforward to quickly and accurately quantify the latent viral load in a sample, e.g., a biological sample from a subject diagnosed as suffering from the virus. Accordingly, the methods allow for faster clinical evaluation of treatments for the virus. The methods also allow health care providers to evaluate the progress of an individual's latent viral load and response to treatment. Thus, some patients may be able to scale back on the amount or type of antiretroviral agents that are administered. This will reduce overall healthcare costs for the population and potentially increase the effectiveness of the antiretroviral agents because the virus will not develop a resistance to the antiretroviral agents as quickly.

Because measurements can be performed on individual droplets, quantification typically only involves counting droplets with and without the targeted properties. For example, the amount of RNA in a sample that is replication competent is quantified. In another embodiment, enzyme molecules are quantified based on their activity inside individual droplets. For example, droplets may be identified as “negative” and/or “positive” droplets for the RNA or the enzyme, and the number of RNA molecules or enzyme molecules within positive droplets may be determined. In other embodiments, the results may not be “digital,” but exhibit a variety of characteristics, e.g., a variety of closely-related sequences and a variety of enzymatic activity. In such instances, it may be necessary to invoke statistical models to deconvolve the results.

The above embodiments and implementations are not necessarily inclusive or exclusive of each other and may be combined in any manner that is non-conflicting and otherwise possible, whether they are presented in association with a same, or a different, embodiment or implementation. The description of one embodiment or implementation is not intended to be limiting with respect to other embodiments and/or implementations. Also, any one or more function, step, operation, or technique described elsewhere in this specification may, in alternative implementations, be combined with any one or more function, step, operation, or technique described in the summary. Thus, the above embodiment and implementations are illustrative rather than limiting.

BRIEF DESCRIPTION OF THE DRAWINGS

The above and further features will be more clearly appreciated from the following detailed description when taken in conjunction with the accompanying drawings. In the drawings, like reference numerals indicate like structures, elements, or method steps and the leftmost digit of a reference numeral indicates the number of the figure in which the references element first appears (for example, element 120 appears first in FIG. 1). All of these conventions, however, are intended to be typical or illustrative, rather than limiting.

FIG. 1 is a functional block diagram of one embodiment of a system for droplet generation and detection;

FIG. 2 is a simplified graphical representation of one embodiment of a droplet generation device of the system of FIG. 1;

FIG. 3 is a simplified graphical representation of one embodiment of a miRNA qPCR detection processes;

FIG. 4 is a simplified graphical representation of one embodiment of one-step RT-PCR results from miR-16 and Xeno assays of Samples A-H;

FIG. 5 is a simplified graphical representation of one embodiment of data comprising droplet counts of the results of FIG. 4;

FIG. 6 is a simplified graphical representation of one embodiment of one-step RT-PCR results from miR-16, miR-21, and miR-92a assays with Xeno spike in for Samples A-F;

FIG. 7 is a simplified graphical representation of one embodiment of one-step RT-PCR results from miR-21 and miR-15, for Samples A-C;

FIG. 8 is a simplified graphical representation of one embodiment of one-step RT-PCR results from endogenous mRNA and miR-21, for Samples A and B;

FIG. 9 is a schematic showing sandwich formation for digital droplet ELISA;

FIGS. 10A-D illustrate different digital droplet ELISA readout counting modes; and

FIG. 11 is a simplified graphical representation of one embodiment of a workflow for encapsulating HIV virions in droplets and incorporating barcode for whole genome sequencing of individual virus.

DETAILED DESCRIPTION

As will be described in greater detail below, embodiments of the described invention include systems and methods for super-efficient reverse transcription and detection of RNA species in a single molecule format. More specifically, embodiments of a unique one step approach are described in detail below that enable highly accurate and quantifiable detection of RNA species such as, but not limited to, small RNA species and viral RNA species. Further, in the described embodiments the RNA species are compartmentalized in droplets prior to amplification which enables massive parallelization of single molecule targets that provide advantages in statistical significance and throughput.

One embodiment of the invention includes super-efficient reverse transcription of virion RNA into a cDNA product and sequencing the cDNA product. Embodiments of the invention additionally include methods for estimation of latent viral loads by detecting an amount of enzyme that is attributable only to the presence of the viral load. For example, certain families of reverse transcriptase are only attributable to the presence of HIV, a retrovirus. Each HIV virion contains 50-100 molecules having enzymatic activity (either RT or RNAseH or both), and these species are also present in the host cell during various stages of the HIV life cycle (i.e. infection or escape from latency). This invention relates to absolute quantification of each individual enzyme molecule confined into separate compartments for a digital counting assay.

For the enzyme quantification methods described, test materials (e.g. cell lysate, culture supernate, etc.) are recovered, diluted, and partitioned to create a single molecule (‘digital’) environment together with additional assay components, enzymatic reaction to a fluorescent endpoint. Once the reactions are complete the latent viral load and be quantified by simply counting ‘positive’ compartments. In some embodiments, the total number of positive compartments will be identical to the total number of starting enzyme molecules present in the measured test fluid, and can be correlated to the number of viral species present. Furthermore, measurement of RT activity can be performed by co-encapsulation with a known substrate (e.g. exogenous RNA) and detection assay (e.g. qPCR assay for the exogenous RNA, or the use of a fluorogenic RNA substrate). Similarly, RNAseH detection would utilize co-encapsulation of a substrate (e.g. synthetic RNA/DNA hybrid) together with a detection assay (e.g. qPCR assay for the exogenousDNA that is released from the RNA/DNA hybrid after RNAseH activity, or the use of a fluorogenic RNA/DNA substrate).

In some embodiments, exogenous or endogenous controls are utilized to improve the accuracy of quantification. For example, a “spike-in” (e.g. an addition from user 101, FIG. 1) nucleic acid (e.g. synthetic control RNA, cDNA, or DNA species) may be added at known concentrations to the sample with target small RNA molecules. In the present example, a microfluidic device can be used to encapsulate the target small RNA and control nucleic acid in droplets that are subjected to a first strand cDNA synthesis step, and in some embodiments an amplification reaction, the cDNA and/or amplification products are then detected in the droplets (e.g. via digital PCR) or released from the droplets and detected (e.g. via sequencing). In the present example, the detected numbers for the spike-in nucleic acid can be compared to the known numbers from the concentration and, if necessary, the detected numbers for the small RNA numbers may be normalized to increase accuracy. Also in the present or different example, an endogenous mRNA target may be utilized together or separately with the exogenous spike-in nucleic acid for additional normalization of comparison.

Some exemplary embodiments of systems and methods associated with sample preparation and processing, generation of data, and analysis of data are generally described below, some or all of which are amenable for use with embodiments of the presently described invention. In particular, the exemplary embodiments of systems and methods for preparation of nucleic acid template molecules, amplification of template molecules, detection of template molecules and/or substantially identical copies thereof. Embodiments that execute methods of detection such as digital PCR and/or sequencing methods utilizing exemplary instrumentation and computer systems are described.

Typical embodiments of “emulsions” include creating a stable emulsion of two immiscible substances, and in the embodiments described herein generally refer to an emulsion of aqueous droplets in a continuous oil phase within which reactions may occur. In particular, the aqueous droplets of an emulsion amenable for use in methods for conducting reactions with biological samples and detecting products may include a first fluid, such as a water based fluid (typically referred to as “aqueous” fluid) suspended or dispersed as droplets (also referred to as a discontinuous phase) within another fluid, such as a hydrophobic fluid (also referred to as a continuous phase) that typically includes some type of oil. Examples of oil that may be employed include, but are not limited to, mineral oils, silicone based oils, fluorinated oils, partially fluorinated oils, or perfluorinated oils.

One example of an aqueous fluid compatible with embodiments of the invention may include an aqueous buffer solution, such as ultrapure water (e.g., 18 mega-ohm resistivity, obtained, for instance by column chromatography), 10 mM Tris HCl and 1 mM EDTA (TE) buffer, phosphate buffer saline (PBS) or acetate buffer. In the presently described example, any liquid or buffer that is physiologically compatible with nucleic acid molecules or encapsulated biological entity can be used. Also, in the same or alternative example a carrier fluid compatible with embodiments of the invention includes a non-polar solvent, decane (eg., tetradecane or hexadecane), fluorocarbon oil, silicone oil or another oil (for example, mineral oil). In certain embodiments, the carrier fluid may contain one or more additives, such as agents which increase, reduce, or otherwise create non-Newtonian surface tensions (surfactants) and/or stabilize droplets against spontaneous coalescence on contact.

Embodiments of surfactants that act to stabilize emulsions, which may be particularly useful for embodiments that include conducting reactions with biological samples such as PCR may include one or more of a silicone or fluorinated surfactant. For example, in microfluidic embodiments the addition of one or more surfactants can aid in controlling or optimizing droplet size, flow and uniformity, for example by reducing the shear force needed to extrude or inject droplets into an intersecting channel. This can affect droplet volume and periodicity, or the rate or frequency at which droplets break off into an intersecting channel. Furthermore, the surfactant can serve to stabilize aqueous emulsions in fluorinated oils and substantially reduce the likelihood of droplet coalescence.

In some embodiments, the aqueous droplets may be coated with a surfactant or a mixture of surfactants, where those of skill in the art understand that surfactant molecules typically reside at the interface between immiscible fluids, and in some cases form micelles in the continuous phase when the concentration of surfactant(s) is greater than what is referred to as the critical micelle concentration (also sometimes referred to as CMC). Examples of surfactants that may be added to the carrier fluid include, but are not limited to, surfactants such as sorbitan-based carboxylic acid esters (e.g., the “Span” surfactants, Fluka Chemika), including sorbitan monolaurate (Span 20), sorbitan monopalmitate (Span 40), sorbitan monostearate (Span 60) and sorbitan monooleate (Span 80), and perfluorinated polyethers (e.g., DuPont Krytox 157 FSL, FSM, and/or FSH). Other non-limiting examples of non-ionic surfactants which may be used include polyoxyethylenated alkylphenols (for example, nonyl-, p-dodecyl-, and dinonylphenols), polyoxyethylenated straight chain alcohols, polyoxyethylenated polyoxypropylene glycols, polyoxyethylenated mercaptans, long chain carboxylic acid esters (for example, glyceryl and polyglycerl esters of natural fatty acids, propylene glycol, sorbitol, polyoxyethylenated sorbitol esters, polyoxyethylene glycol esters, etc.) and alkanolamines (e.g., diethanolamine-fatty acid condensates and isopropanolamine-fatty acid condensates).

In one embodiment, a fluorosurfactant can be prepared by reacting the perflourinated polyether DuPont Krytox 157 FSL, FSM, or FSH with aqueous ammonium hydroxide in a volatile fluorinated solvent. The solvent and residual water and ammonia can be removed with a rotary evaporator. The surfactant can then be dissolved (e.g., 2.5 wt %) in a fluorinated oil (e.g., Flourinert (3M)), which then serves as the carrier fluid (e.g. continuous phase). In the presently described embodiment, the surfactant produced is an ionic salt, and it will be appreciated that other embodiments of non-ionic surfactant compositions may also be used. For example, non-ionic surfactant composition may include what are referred to as block copolymers (e.g. di-block, or tri-block copolymers) typically comprising a head group and one or more tail groups. A more specific example of a fluorinated block copolymer includes a polyethylene glycol (PEG) head group and one or more perfluoropolyether (PFPE) tail groups.

Further, in some embodiments other reagents that act as droplet stabilizers (also referred to as passivating agents) may be included. Useful droplet stabilizing reagents may include, but are not limited to, polymers, proteins, BSA, spermine, or PEG.

In some embodiments, desirable characteristics may be achieved by adding a second surfactant, or other agent, such as a polymer or other additive, to the aqueous fluid. Further, in certain embodiments utilizing microfluidic technology the carrier fluid may be caused to flow through the outlet channel so that the surfactant in the carrier fluid coats the channel walls.

In the embodiments described herein, droplets of an emulsion may be referred to as compartments, microcapsules, microreactors, microenvironments, or other name commonly used in the related art. The aqueous droplets may range in size depending on the composition of the emulsion components or composition, contents contained therein, and formation technique employed. The described emulsions are microenvironments within which chemical reactions that may include binding reactions, such as Reverse Transcription, PCR, or other process may be performed. For example, template nucleic acids and all reagents necessary to perform a desired PCR reaction may be encapsulated and chemically isolated in the droplets of an emulsion. Additional surfactants or other stabilizing agent may be employed in some embodiments to promote additional stability of the droplets as described above. Thermocycling operations typical of PCR methods may be executed using the droplets to amplify an encapsulated nucleic acid template resulting in the generation of a population comprising many substantially identical copies of the template nucleic acid. In some embodiments, the population within the droplet may be referred to as a “clonally isolated”, “compartmentalized”, “sequestered”, “encapsulated”, or “localized” population. Also in the present example, some or all of the described droplets may further encapsulate a solid substrate such as a bead. In some embodiments, beads may be employed for attachment of template and amplified copies of the template, amplified copies complementary to the template, or combination thereof. Further, the solid substrate may be enabled for attachment of other type of nucleic acids, reagents, labels, or other molecules of interest. It will also be appreciated that the embodiments described herein are not limited to encapsulating nucleic acids in droplets, but rather the droplets may be configured to encapsulate a variety of entities that include, but are limited to, cells, antibodies, enzymes, proteins, or combinations thereof. As with nucleic acids, the droplets may further be amenable to performing various reactions on the entities encapsulated therein and/or detection methods such as, for instance, ELISA assays.

Various methods of forming emulsions may be employed with the described embodiments. In the some embodiments methods involve forming aqueous droplets where some droplets contain zero target nucleic acid molecules, some droplets contain one target nucleic acid molecule, and some droplets may contain multiple target nucleic acid molecules. It will be appreciated by those of skill in the art that in some embodiments it may be desirable for individual droplets to contain multiple nucleic acid molecules from a sample, however in certain assays there may be a discrete number of targets of interest where droplets are generated based on the likelihood that there is at most a single target of interest in each droplet in the presence of other nucleic acid molecules that are not targets of interest.

In some embodiments the number of target nucleic acid molecules in the droplets is controlled via a limiting dilution of the target nucleic acid molecules in the aqueous solution. Alternatively, in some embodiments the number of target nucleic acid molecules in the droplets is controlled via a method of partitioning very small volumes of the aqueous fluid (e.g. picoliter—nanoliter volumes such as a volume of about 5 picoliters) into the droplet where the statistical likelihood of distributing multiple target nucleic acid molecules in the same droplet is very small. In some or all of the described embodiments, the distribution of molecules within droplets can be described by Poisson distribution. However, it will be appreciated that methods for non-Poisson loading of droplets may be employed in some embodiments and include, but are not limited to, active sorting of droplets such as by laser-induced fluorescence, or by passive one-to-one loading.

Systems and methods for generation of emulsions include what are referred to as “bulk” emulsion generation methods that generally include an application of energy to a mixture of aqueous and carrier fluids. In the example of bulk generation methods energy may be applied by agitation via vortexing, shaking, spinning a paddle (to create shear forces) in the combined mixture or in some embodiments the agitation of the aqueous solution may applied when separate from the immiscible fluid where the agitation results in droplets being added to the immiscible fluid as for example when piezo-electric agitation is employed. Alternatively, some bulk generation methods include adding the aqueous fluid drop-wise to a spinning carrier fluid. Bulk emulsion generation methods typically produce emulsions very quickly and do not require complicated or specialized instrumentation. The droplets of the emulsions generated using bulk generation techniques typically have low uniformity with respect to dimension and volume of the droplets in the emulsion.

Other embodiments of emulsion formation methods include “microfluidic” based formation methods that may employ a junction of channels carrying aqueous and carrier fluids that result in an output of droplets in a stream of flow. Some embodiments of microfluidic based droplet generation approaches may utilize one or more electric fields to overcome surface tension. Alternatively, some embodiments do not require the addition of an electric field. For example, a water stream can be infused from one channel through a narrow constriction; counter propagating oil streams (preferably fluorinated oil) hydrodynamically focus the water stream and stabilize its breakup into droplets as it passes through the constriction. In order to form droplets, the viscous forces applied by the oil to the water stream must overcome the water surface tension. The generation rate, spacing and size of the water droplets is controlled by the relative flow rates of the oil and the water streams and nozzle geometry. While this emulsification technology is extremely robust, droplet size and rate are tightly coupled to the fluid flow rates and channel dimensions.

Continuing with the present example, some embodiments of microfluidic devices can incorporate integrated electric fields, thereby creating an electrically addressable emulsification system. For instance, this can be achieved by applying high voltage to the aqueous stream and charge the oil water interface. The water stream behaves as a conductor while the oil is an insulator; electrochemical reactions charge the fluid interface like a capacitor. At snap-off, charge on the interface remains on the droplet. The droplet size decreases with increasing field strength. At low applied voltages the electric field has a negligible effect, and droplet formation is driven exclusively by the competition between surface tension and viscous flow

Additional examples of systems and methods for forming aqueous droplets surrounded by an immiscible carrier fluid in microfluidic structures are described U.S. Pat. Nos. 7,708,949; and 7,041,481 (reissued as RE 41,780) and U.S. Published Patent Application numbers 2006/0163385 A1; 2008/0014589; 2008/0003142; and 2010/0137163; and 2010/0172803 each of which is hereby incorporated by reference herein in its entirety for all purposes.

In some embodiments, emulsion formation methods also include merging already formed emulsion droplets with other droplets or streams of fluid to produce combined droplets. The merging of droplets can be accomplished using, for example, one or more droplet merging techniques described for example in Link et al. (U.S. patent application numbers 2008/0014589; 2008/0003142; and 2010/0137163) and European publication number EP2047910 to RainDance Technologies Inc.

In certain embodiments, a reverse transcriptase reaction (referred to as an “RT” reaction) may be used to convert from RNA starting material to a nucleic acid such as cDNA or other synthetic nucleic acid derivative. Reverse transcriptase reaction refers to methods known in the art, for example by methods described by Yih-Horng Shiao, (BMC Biotechnology 2003, 3:22; doi:10.1186/1472-6750-3-22). See also J Biomol Tech. 2003 March; 14(1): 33-43, which includes a discussion of RT reaction methods, each of which is incorporated by reference. For example, the process includes a first step of introducing a reverse transcriptase enzyme used to generate single stranded complementary DNA (cDNA) from an RNA template using target- specific primers (sometimes referred to as “RT primers”) or random hexamers. For embodiments of conversion of small RNA to cDNA a target-specific stem loop primer may be used to add length and optimize characteristics such as melting temperature and specificity. In some embodiments, the single stranded cDNA is then used as a template for conversion of a second strand complementary to the single stranded cDNA. The single or double stranded cDNA may then be used as a template for amplification, such as by PCR. The process for amplifying the target sequence can include introducing an excess of oligonucleotide primers to a DNA or cDNA mixture containing a desired target sequence, followed by a precise sequence of thermal cycling in the presence of a DNA polymerase. The primers are complementary to their respective strands of the double stranded target sequence.

As described elsewhere in this description, the described embodiments include conducting reactions with biological entities within the emulsion droplets. An example of a very useful class of reactions includes nucleic acid amplification methods. The term “amplification” as used herein generally refers to the production of substantially identical copies of a nucleic acid sequence (typically referred to as “amplicons”). One of the most well-known amplification strategies is the polymerase chain reaction (e.g., Dieffenbach and Dveksler, PCR Primer, a Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y. [1995]). The amplification reaction may include any amplification reaction known in the art that amplifies nucleic acid molecules, such as Loop-mediated Isothermal Amplification (also referred to as LAMP), Recombinase Polymerase Amplification (RPA), Helicase-dependent amplification (HDA), Nicking enzyme amplification reaction (NEAR), polymerase chain reaction, nested polymerase chain reaction, ligase chain reaction (Barany F. (1991) PNAS 88:189-193; Barany F. (1991) PCR Methods and Applications 1:5-16), ligase detection reaction (Barany F. (1991) PNAS 88:189-193), strand displacement amplification (SDA), transcription based amplification system, nucleic acid sequence-based amplification, rolling circle amplification, and hyper-branched rolling circle amplification.

In some embodiments, generally referred to as “multiplexing”, emulsion droplets comprise a plurality of species of primer pairs each specific to amplify a different region of nucleic acid sequence. Optimization of traditional multiplexing of standard PCR primers in tubes or wells is known to be difficult. Multiple PCR amplicons being generated in the same reaction can lead to competition between amplicons that have differing efficiencies due to differences in sequence or length or access to limiting reagents. This results in varying yields between competing amplicons which can result in non-uniform amplicon yields. However, because droplet based digital amplification utilizes only one template molecule per droplet, even if there are multiple PCR primer pairs present in the droplet, only one primer pair will be active. Since only one amplicon is being generated per droplet, there is no competition between amplicons or reagents, resulting in a more uniform amplicon yield between different amplicons.

In some embodiments, even though the number of PCR primer pairs per droplet is greater than one, there is still at most only one template molecule per droplet and thus there is only one primer pair per droplet that is being utilized at one time. This means that the advantages of droplet amplification for eliminating bias from either allele specific PCR or competition between different amplicons is maintained.

Additional examples describing systems and methods for performing amplification in droplets are shown for example in Link et al. (U.S. patent application numbers 2008/0014589, 2008/0003142, and 2010/0137163), Anderson et al. (U.S. Pat. No. 7,041,481 and which reissued as RE 41,780) and European publication number EP2047910 to RainDance Technologies Inc. The content of each of which is incorporated by reference herein in its entirety.

In certain cases it is desirable to release the contents of the droplets to use in further processing and/or detection processes. In some embodiments, the contents of many droplets are released and pooled together, however it will be appreciated that in some embodiments the contents of droplets are released individually and maintained separately. Various methods for releasing the contents of droplets may be employed, typically depending on the composition of the droplets. For example, in cases where aqueous droplets are in a silicone based oil, an organic solvent may be used to “break” the integrity of the interface between the aqueous fluid and silicone oil combining into a single solution that may be separated using various techniques. Alternatively, in cases where aqueous droplets are in a fluorinated oil, a perfluorinated alcohol reagent may be used. In the present example, the perfluorinated alcohol provides advantages for use as a releasing agent in that it is not immiscible with aqueous fluid (e.g. will not be present in aqueous phase post release) and works very well to disrupt surfactants typically used with fluorinated oils. One specific example of perfluorinated alcohol useful for release applications includes perfluoro decanol.

In some embodiments, often referred to as digital PCR, after amplification the emulsion droplets are introduced into an instrument for optical detection of amplification products. In some embodiments the generation and amplification of the nucleic acid molecules occurs in a single fluidic chip that is also used for detection, alternatively the emulsion droplets may be removed or dispensed from a fluidic chip used for droplet generation in order to conduct the amplification “off-chip”. For embodiments of the off-chip application, post amplification the droplets may be introduced into either a second fluidic chip used for detection of the amplicons or into the original fluidic chip used for droplet generation. Further, in embodiments where the emulsion droplets are generated using bulk methods, after amplification the droplets may be introduced into a fluidic chip used for detection of amplicon products. In the same or alternative embodiments detection of reaction products produced from PCR thermocycling may be performed during or after each amplification cycle (e.g. sometimes referred to as “real time” PCR). The detected signals from the reaction products may be used to generate what are referred to as “melt curves” sometimes used with known concentrations as standards for calibration. Melt curves may also be based on the melting temperature of probes in the reaction where combinations of probes are associated with specific sequence composition of a target (e.g. as an identifier or type of molecular barcode) where the presence of the target can be identified from the melt curve signature.

In some embodiments, when droplets are introduced into a fluidic chip used for detection it may be highly desirable to add additional carrier fluid to increase the spacing between successive droplets. Examples of increasing the spacing between droplets is described in U.S. patent application Ser. No. 12/087,713 which is hereby incorporated by reference herein in its entirety for all purposes.

The emulsion droplets may be individually analyzed and detected using any methods known in the art, such as detecting the presence and/or amount of signal from a reporter. Generally, the instrument for detection comprises one or more detection elements. The detection elements can be optical, magnetic, electromagnetic, or electrical detectors, other detectors known in the art, or combinations thereof. Examples of suitable detection elements include optical waveguides, microscopes, diodes, light stimulating devices, (e.g., lasers), photo multiplier tubes, charge-coupled devices (CCD), and processors (e.g., computers and software), and combinations thereof, which cooperate to detect a signal representative of a characteristic, marker, or reporter. Further description of detection instruments and methods of detecting amplification products in droplets are shown in Link et al. (U.S. patent application numbers 2008/0014589, 2008/0003142, and 2010/0137163) and European publication number EP2047910 to RainDance Technologies Inc., each of which is hereby incorporated by reference herein in its entirety for all purposes.

In certain embodiments, amplified target nucleic acid molecules are detected using detectably labeled probes, such as hybridization probes. In some or all of the described embodiments a probe type may comprise a plurality of probes that recognize a specific nucleic acid sequence composition. For example, a probe type may comprise a group of probes that recognize the same nucleic acid sequence composition where the members of the group have one or more detectable labels specific for that probe type and/or members that do not include a detectable label (that may be included to modulate intensity of reporter signal). Further the probe members may be present at different concentrations relative to each other within the droplets. Thus, the combination of detectable labels and relative intensities detected from the concentrations of probes are specific to and enable identification of the probe type. Those of ordinary skill in the related art appreciate that the embodiments described herein are compatible with any type of fluorogenic DNA hybridization probes or hydrolysis probes, such as TaqMan probes, molecular beacons, Solaris probes, scorpion probes, and any other probes that function by sequence specific recognition of target DNA by hybridization and result in increased fluorescence on amplification of the target sequence. Further in the embodiments described herein, probe types may also be multiplexed in emulsion droplets in the same way as described elsewhere with respect to multiplexing primer species.

As described elsewhere, the droplets may contain a plurality of detectable probes that hybridize to amplicons produced in the droplets. Members of the plurality of probes can each include the same detectable label, or a different detectable label. The plurality of probes can also include one or more groups of probes at varying concentration. The groups of probes at varying concentrations can include the same detectable label which varies in intensity, due to varying probe concentrations. In the embodiments described herein, the fluorescence emission from each fused droplet may be determined and plotted on a scattered plot based on its wavelength and intensity. Examples of probe detection and analysis using wavelength and intensity is described in US Patent Application Serial No 2011/0250597, which is hereby incorporated by reference herein in its entirety for all purposes.

Types of detectable labels suitable for use with probes specific to bridge regions of a primer and other probes for use in methods of the invention are described hereinafter. In some embodiments, the detectably labeled probes are optically labeled probes, such as fluorescently labeled probes. Examples of fluorescent labels include, but are not limited to, Atto dyes, 4-acetamido-4′-isothiocyanatostilbene-2,2′disulfonic acid; acridine and derivatives: acridine, acridine isothiocyanate; 5-(2′-aminoethyl)aminonaphthalene-1-sulfonic acid (EDANS); 4-amino-N-[3-vinylsulfonyl)phenyl]naphthalimide-3,5 disulfonate; N-(4-anilino-1-naphthyl)maleimide; anthranilamide; BODIPY; Brilliant Yellow; coumarin and derivatives; coumarin, 7-amino-4-methylcoumarin (AMC, Coumarin 120), 7-amino-4-trifluoromethylcouluarin (Coumaran 151); cyanine dyes; cyanosine; 4′,6-diaminidino-2-phenylindole (DAPI); 5′5″-dibromopyrogallol-sulfonaphthalein (Bromopyrogallol Red); 7-diethylamino-3-(4′-isothiocyanatophenyl)-4-methylcoumarin; diethylenetriamine pentaacetate; 4,4′-diisothiocyanatodihydro-stilbene-2,2′-disulfonic acid; 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid; 5-[dimethylamino]naphthalene-1-sulfonyl chloride (DNS, dansylchloride); 4-dimethylaminophenylazophenyl-4′-isothiocyanate (DABITC); eosin and derivatives; eosin, eosin isothiocyanate, erythrosin and derivatives; erythrosin B, erythrosin, isothiocyanate; ethidium; fluorescein and derivatives; 5-carboxyfluorescein (FAM), 5-(4,6-dichlorotriazin-2-yl)aminofluorescein (DTAF), 2′,7′-dimethoxy-4′5′-dichloro-6-carboxyfluorescein, fluorescein, fluorescein isothiocyanate, QFITC, (XRITC); fluorescamine; IR144; IR1446; Malachite Green isothiocyanate; 4-methylumbelliferoneortho cresolphthalein; nitrotyrosine; pararosaniline; Phenol Red; B-phycoerythrin; o-phthaldialdehyde; pyrene and derivatives: pyrene, pyrene butyrate, succinimidyl 1-pyrene; butyrate quantum dots; Reactive Red 4 (Cibacron™ Brilliant Red 3B-A) rhodamine and derivatives: 6-carboxy-X-rhodamine (ROX), 6-carboxyrhodamine (R6G), lissamine rhodamine B sulfonyl chloride rhodamine (Rhod), rhodamine B, rhodamine 123, rhodamine X isothiocyanate, sulforhodamine B, sulforhodamine 101, sulfonyl chloride derivative of sulforhodamine 101 (Texas Red); N,N,N′,N′tetramethyl-6-carboxyrhodamine (TAMRA); tetramethyl rhodamine; tetramethyl rhodamine isothiocyanate (TRITC); riboflavin; rosolic acid; terbium chelate derivatives; Cy3; Cy5; Cy5.5; Cy7; IRD 700; IRD 800; La Jolta Blue; phthalo cyanine; and naphthalo cyanine. Preferred fluorescent labels for certain embodiments include FAM and VIC, and in the same or alternative embodiments may also include TET, Yakima yellow, Calcein orange, ABY and JUN dyes (from Thermo Fisher Scientific). Labels other than fluorescent labels are contemplated by the invention, including other optically-detectable labels.

Additional examples of digital amplification and detection of reporters are described in U.S. Pat. No. 8,535,889, which is hereby incorporated by reference herein in its entirety for all purposes.

In embodiments of digital PCR, data analysis typically involves a scatter plot type of representation for identifying and characterizing populations of statistically similar droplets that arise from unique probe signatures (wavelength and intensity), and for discriminating one population of droplets from the others. In some embodiments, a user and/or computer application may select data points associated with specific droplets or groups of droplets within histograms, either for counting, or for assay selection as in the use of optical labels, or for any other purpose. Some methods of selection may include the application of boundaries surrounding one or more selections, either closed or unclosed, of any possible shape and dimension.

The embodiments described herein are not limited to the use of a specific number of probe species. In some embodiments a plurality of probe species are used to give additional information about the properties of nucleic acids in a sample. For example, three probe species could be used wherein a first probe species comprises a fluorophore that has a particular excitation and emission spectra (e.g., VIC), and a second probe species comprises a fluorophore that has a particular excitation and emission spectra (e.g., FAM) where the excitation spectra for the first and second probe species may overlap but have clearly distinct emission spectra from each other. Detected differences in intensity can be used to discriminate between different probe species that employ the same fluorophore, where the intensity may be tunable of emitted light.

In some of the described embodiments, a further step of releasing converted or amplified target molecules from the emulsion droplets for further analysis. The released converted or amplified material can also be subjected to further processing and/or amplification. Additional examples of systems and methods of releasing amplified target molecules from the droplets are described in Link et al. (U.S. patent application numbers 2008/0014589, 2008/0003142, and 2010/0137163) and European publication number EP2047910 to RainDance Technologies Inc.

In certain embodiments, the amplified target molecules are sequenced using any suitable sequencing technique known in the art. In one example, the sequencing is single-molecule sequencing-by-synthesis. Single-molecule sequencing is shown for example in Lapidus et al. (U.S. Pat. No. 7,169,560), Quake et al. (U.S. Pat. No. 6,818,395), Harris (U.S. Pat. No. 7,282,337), Quake et al. (U.S. patent application number 2002/0164629), and Braslaysky, et al., PNAS (USA), 100: 3960-3964 (2003), the contents of each of these references is incorporated by reference herein in its entirety. Other examples of sequencing nucleic acids may include Maxam-Gilbert techniques, Sanger type techniques, Sequencing by Synthesis methods (SBS), Sequencing by Hybridization (SBH), Sequencing by Ligation (SBL), Sequencing by Incorporation (SBI) techniques, massively parallel signature sequencing (MPSS), polony sequencing techniques, nanopore, waveguide and other single molecule detection techniques, reversible terminator techniques, or other sequencing technique now know or may be developed in the future.

In one embodiment, the sequencing is Illumina sequencing. Illumina sequencing is based on the amplification of DNA on a solid surface using fold-back PCR and anchored primers. Genomic DNA is fragmented, and adapters are added to the 5′ and 3′ ends of the fragments. DNA fragments that are attached to the surface of flow cell channels are extended and bridge amplified. The fragments become double stranded, and the double stranded molecules are denatured. Multiple cycles of the solid-phase amplification followed by denaturation can create several million clusters of approximately 1,000 copies of single-stranded DNA molecules of the same template in each channel of the flow cell. Primers, DNA polymerase and four fluorophore-labeled, reversibly terminating nucleotides are used to perform sequential sequencing. After nucleotide incorporation, a laser is used to excite the fluorophores, and an image is captured and the identity of the first base is recorded. The 3′ terminators and fluorophores from each incorporated base are removed and the incorporation, detection and identification steps are repeated.

In another embodiment, Ion Torrent sequencing can be used. (See, e.g., U.S. patent application numbers 2009/0026082, 2009/0127589, 2010/0035252, 2010/0137143, 2010/0188073, 2010/0197507, 2010/0282617, 2010/0300559), 2010/0300895, 2010/0301398, and 2010/0304982), the content of each of which is incorporated by reference herein in its entirety.) Oligonucleotide adaptors are ligated to the ends of target nucleic acid molecules. The adaptors serve as primers for amplification and sequencing of the fragments. The fragments can be attached to a surface and is attached at a resolution such that the fragments are individually resolvable. Addition of one or more nucleotides releases a proton (H+), which signal detected and recorded in a sequencing instrument. The signal strength is proportional to the number of nucleotides incorporated.

Embodiments of a typical fluidics based droplet digital amplification platform generally include one or more instrument elements employed to execute one or more process steps. FIG. 1 provides an illustrative example of droplet system 100 constructed and arranged to generate droplets containing templates, amplification of the templates, and detection of the amplified products. In some embodiments, droplet system 100 includes droplet generation instrument 110, thermocycler instrument 115, and droplet detection instrument 120, although it will be appreciated that operations may be combined into a single instrument depending on the number and nature of process steps. Importantly, user 101 may include any type of user of droplet amplification technologies.

Also in the same or alternative embodiments, droplet system 100 comprises sequencing instrument 130 that may include a subsystem that operatively couples a reaction substrate to a particular mode of data capture (i.e. optical, temperature, pH, electric current, electrochemical, etc.), one or more data processing elements, and a fluidic subsystem that enables execution of sequencing reactions on the reaction substrate. For example, some embodiments of detectors for fluorescence readout may include conventional epifluorescence microscopy with a custom microscope.

Further, as illustrated in FIG. 1, droplet system 100 may be operatively linked to one or more external computer components, such as computer 150 that may, for instance, execute system software or firmware, such as application 155 that may provide instructional control of one or more of the instruments, such as droplet generation instrument 110, thermocycler instrument 115, droplet detection instrument 120, sequencing instrument 130, and/or signal processing/data analysis functions. Computer 150 may be additionally operatively connected to other computers or servers via network 180 that may enable remote operation of instrument systems and the export of large amounts of data to systems capable of storage and processing. Also in some embodiments network 180 may enable what is referred to as “cloud computing” for signal processing and/or data analysis functions. In the present example, droplet system 100 and/or computer 130 may include some or all of the components and characteristics of the embodiments generally described herein.

FIG. 2 provides an illustrative example of droplet generator 200. Droplet generation instrument 110 typically includes one or more embodiments of droplet generator 200, where in some embodiments it is highly desirable to have multiple embodiments of droplet generator 200 that operate in parallel to substantially increase the rate of droplet generation. In the present example, droplet generator 200 includes inlet channel 201, outlet channel 202, and two carrier fluid channels 203 and 204. Channels 201, 202, 203, and 204 meet at a junction 205. Inlet channel 201 flows sample fluid to junction 205. Carrier fluid channels 203 and 204 flow a carrier fluid that is immiscible with the sample fluid to junction 205. Inlet channel 201 narrows at its distal portion wherein it connects to junction 205. Inlet channel 201 is oriented to be perpendicular to carrier fluid channels 203 and 204. As described elsewhere, droplets are formed as sample fluid flows from inlet channel 201 to junction 205, where the sample fluid interacts with flowing carrier fluid provided to the junction 205 by carrier fluid channels 203 and 204. Outlet channel 202 receives the droplets of sample fluid surrounded by carrier fluid.

An exemplary embodiment of a computer system for use with the presently described invention may include any type of computer platform such as a workstation, a personal computer, a server, or any other present or future computer. It will, however, be appreciated by one of ordinary skill in the art that the aforementioned computer platforms as described herein are specifically configured to perform the specialized operations of the described invention and are not considered general purpose computers, although the specialized computer platforms may also be capable of performing operations typical of general purpose computers. Computers typically include known components, such as a processor, an operating system, system memory, memory storage devices, input-output controllers, input-output devices, and display devices. It will also be understood by those of ordinary skill in the relevant art that there are many possible configurations and components of a computer and may also include cache memory, a data backup unit, and many other devices.

Display devices may include equipment that provides visual information, this information typically may be logically and/or physically organized as an array of pixels. An interface controller may also be included that may comprise any of a variety of known or future software programs for providing input and output interfaces. For example, interfaces may include what are generally referred to as “Graphical User Interfaces” (often referred to as GUI's) that provides one or more graphical representations to a user. Interfaces are typically enabled to accept user inputs using means of selection or input known to those of ordinary skill in the related art.

In the same or alternative embodiments, applications on a computer may employ an interface that includes what are referred to as “command line interfaces” (often referred to as CLI's). CLI's typically provide a text based interaction between an application and a user. Typically, command line interfaces present output and receive input as lines of text through display devices. Those of ordinary skill in the related art will appreciate that interfaces may include one or more GUI's, CLI's or a combination thereof.

A processor may include a commercially available processor or a processor that are or will become available. Some embodiments of a processor may include what is referred to as Multi-core processor and/or be enabled to employ parallel processing technology in a single or multi-core configuration. For example, a multi-core architecture typically comprises two or more processor “execution cores”. In the present example, each execution core may perform as an independent processor that enables parallel execution of multiple threads. In addition, those of ordinary skill in the related will appreciate that a processor may be configured in what is generally referred to as 32 or 64 bit architectures, or other architectural configurations now known or that may be developed in the future.

A processor typically executes an operating system that interfaces with firmware and hardware in a well-known manner, and facilitates the processor in coordinating and executing the functions of various computer programs that may be written in a variety of programming languages. An operating system, typically in cooperation with a processor, coordinates and executes functions of the other components of a computer. An operating system also provides scheduling, input-output control, file and data management, memory management, and communication control and related services, all in accordance with known techniques.

System memory may include any of a variety of known or future memory storage devices. Examples include any commonly available random access memory (RAM), magnetic medium, such as a resident hard disk or tape, an optical medium such as a read and write compact disc, or other memory storage device. Memory storage devices may include any of a variety of known or future devices, including a compact disk drive, a tape drive, a removable hard disk drive, USB or flash drive, or a diskette drive. Such types of memory storage devices typically read from, and/or write to, a program storage medium such as, respectively, a compact disk, magnetic tape, removable hard disk, USB or flash drive, or floppy diskette. Any of these program storage media, or others now in use or that may later be developed, may be considered a computer program product. As will be appreciated, these program storage media typically store a computer software program and/or data. Computer software programs, also called computer control logic, typically are stored in system memory and/or the program storage device used in conjunction with memory storage device.

In some embodiments, a computer program product is described comprising a computer usable medium having control logic (computer software program, including program code) stored therein. The control logic, when executed by a processor, causes the processor to perform functions described herein. In other embodiments, some functions are implemented primarily in hardware using, for example, a hardware state machine. Implementation of the hardware state machine so as to perform the functions described herein will be apparent to those skilled in the relevant arts.

Input-output controllers could include any of a variety of known devices for accepting and processing information from a user, whether a human or a machine, whether local or remote. Such devices include, for example, modem cards, wireless cards, network interface cards, sound cards, or other types of controllers for any of a variety of known input devices. Output controllers could include controllers for any of a variety of known display devices for presenting information to a user, whether a human or a machine, whether local or remote. In the presently described embodiment, the functional elements of a computer communicate with each other via a system bus. Some embodiments of a computer may communicate with some functional elements using network or other types of remote communications.

As will be evident to those skilled in the relevant art, an instrument control and/or a data processing application, if implemented in software, may be loaded into and executed from system memory and/or a memory storage device. All or portions of the instrument control and/or data processing applications may also reside in a read-only memory or similar device of the memory storage device, such devices not requiring that the instrument control and/or data processing applications first be loaded through input-output controllers. It will be understood by those skilled in the relevant art that the instrument control and/or data processing applications, or portions of it, may be loaded by a processor in a known manner into system memory, or cache memory, or both, as advantageous for execution.

Also, a computer may include one or more library files, experiment data files, and an internet client stored in system memory. For example, experiment data could include data related to one or more experiments or assays such as detected signal values, or other values associated with one or more experiments or processes. Additionally, an internet client may include an application enabled to accesses a remote service on another computer using a network and may for instance comprise what are generally referred to as “Web Browsers”. Also, in the same or other embodiments an internet client may include, or could be an element of, specialized software applications enabled to access remote information via a network such as a data processing application for biological applications.

A network may include one or more of the many various types of networks well known to those of ordinary skill in the art. For example, a network may include a local or wide area network that may employ what is commonly referred to as a TCP/IP protocol suite to communicate. A network may include a network comprising a worldwide system of interconnected computer networks that is commonly referred to as the internet, or could also include various intranet architectures. Those of ordinary skill in the related arts will also appreciate that some users in networked environments may prefer to employ what are generally referred to as “firewalls” (also sometimes referred to as Packet Filters, or Border Protection Devices) to control information traffic to and from hardware and/or software systems. For example, firewalls may comprise hardware or software elements or some combination thereof and are typically designed to enforce security policies put in place by users, such as for instance network administrators, etc.

Embodiments of the Presently Described Invention

As described above, embodiments of the described invention relate to systems and methods for super-efficient reverse transcription and detection of RNA species in a single target molecule format. Importantly, it is the super-efficient nature of the reverse transcription in the single molecule format that that enables the reduction of user intervention required while reducing background noise. In general, embodiments of the invention enable accurate detection of multiple species of small RNA, mRNA, viral RNA, and other RNA or DNA that may be digitally counted (or detected by sequencing, arrays, or other methods) to provide a quantitative measure of the presence and/or absence of RNA targets. This further enables the generation of a profile of the RNA targets to aid in disease identification, for pre-clinical and clinical investigations.

The term “one step” as used herein generally refers to the number of user intervention steps where, for example, in the embodiments described herein user intervention is not required after droplet generation in order to generate a detectable product from RNA. Importantly, the one-step process compartmentalizes an RNA template and reagents in a single compartment and without any transfer steps that can introduce contamination and loss. FIG. 3 provides an illustrative example of a typical process that requires multiple user intervention steps for reverse transcription and amplification of miRNA.

As described above, some embodiments of the invention provide systems and methods for quantifying multiple species of a sample's RNA molecules (e.g. miRNA, siRNA, piRNA, ceRNA (competing endogenous RNA), saRNA (small activating RNA), other non-coding RNA, mRNA, viral RNA) by first compartmentalizing target RNA molecules into a collection of fluid compartments, such that most of the compartments contain either zero or one target molecules (e.g. a ‘digital format’ or ‘single target molecule format’ or ‘single-molecule-format’) together with the enzymes, primers, probes, and reagents to perform one-step cDNA synthesis and amplification and detection within each droplet. Typical droplets are aqueous droplets surrounded by an immiscible fluid, such as oil, fluorinated oil or other non-immiscible fluid.

Those of ordinary skill in the related art appreciate that the embodiments of the presently described invention are amenable for use with combinations of nucleic acid that may exist in the same sample, such as for example RNA, cDNA, DNA, or other nucleic acid or synthetic nucleic acid now known or developed in the future.

In the embodiments described herein, RNA species are compartmentalized in droplets, converted to first strand cDNA (in some embodiments a second strand may also be synthesized to produce a cDNA duplex molecule) and detected in the droplets and/or released from the droplets and detected in bulk or additional droplet single-molecule formatted assays. In some embodiments the cDNA may be amplified in the droplets to produce many substantially identical copies of the RNA that may increase the level of detectable signal desirable for some applications such as sequencing and/or dPCR. For example, the droplets may include an oligonucleotide probe that is complementary to the cDNA made from a small RNA (and/or the substantially identical DNA copies of the small RNA) and includes a detectable reporter. In one embodiment a detectable reporter may include what is generally referred to as a TaqMan probe that comprises a quencher molecule and a fluorescent reporter molecule, or in the same or alternative embodiments what is generally referred to as an EvaGreen dye may be used. In the example of TaqMan, the fluorescent reporter molecule may be separated from the quencher molecule during an amplification process where the fluorescent signal emitted in response to an excitation light becomes detectable. Other embodiments utilize detection by sequencing or any other method (e.g. array).

The embodiments described herein provide substantial benefits over previous approaches due to the negligible background signal produced and super-efficient reverse transcription of RNA into ‘first-strand’ cDNA, ‘second strand’ cDNA synthesis, amplification, and fluorescence generation (e.g. probe hydrolysis, dye intercalation) of target RNA molecules accomplished in the present invention by employing a one-step method in droplets. The very low background signal produced is likely attributed to the very small volumes provided by the droplets that reduce the likelihood of self-priming by the RT or stem loop primers. This is a very important aspect of the described embodiments due to the fact that background noise is a significant source of error that inhibits the ability to effectively discriminate a true signal. Moreover, differences in RT or qPCR efficiencies do not affect the quantification of target RNA species as long as a sufficient difference between background and signal is present at the amplification endpoint.

Also, full length transcripts generated from the initial encapsulated single target RNA template are generated within the isolated compartment, enabling any incomplete RT to complete (i.e. falling off and subsequent re-hybridization) without the chance to encounter a different target template molecule (no ‘strand switching’). Thus there will be fidelity for any splice variants to be quantified and detected. For example, the super-efficient approach to cDNA synthesis from RNA in droplets as described herein allows the generation of cDNA molecules that are representative of the actual number of target RNA molecules. The cDNA molecules may be directly counted and quantified or amplified to generate substantially identical products that may be quantified or sequenced.

In the described embodiments either the single or double stranded cDNA synthesized from small RNA in the droplets are present at a substantially 1:1 relationship to the original number of small RNA targets and in some embodiments can be counted without further amplification to produce a true digital representation of the amount of small RNA present in the sample. For example, in some embodiments an identifier, such as a barcode sequence, fluorescent moiety, or other reporter known in the related art, may be incorporated into the cDNA during the cDNA synthesis step. In the same or alternative example, what is referred to as Radio Frequency Identification (often referred to as RFID) that receives a signal and transmits information over a short distance and may be used by coupling an RFID tag to the cDNA molecule in a droplet, followed by detection.

In the event that self-priming or other events distort the apparent number of small RNA molecules, a droplet can be discarded or ignored whereas in bulk analysis such events tend to contaminate the entire sample. Thus, the described embodiments reduce biases that are often introduced when carried out in a bulk reaction. Also in the present example, components of total RNA, such as rRNA, tRNA, or other RT or PCR inhibitor may additionally inhibit cDNA generation and/or amplification efficiency by competing for reagents and producing undesired products, where such effects are similarly reduced by the droplet environment (e.g. volume).

Also as described above, in some embodiments exogenous or endogenous controls are utilized to improve the accuracy of quantification. As described elsewhere, an exogenous control may include nucleic acid added by a user (e.g. “spiked-in”) that may not be naturally present in the sample or occurs at a level where it is still useful as a reference. For example, an endogenous mRNA target known to be present in the sample with the RNA targets may be detected using the same method as used to detect the RNA. The concentration of the mRNA present in the sample may be known or unknown and used as a relative measure to the quantity of RNA detected. In the present example, use of the endogenous mRNA as a control may be advantageous for some diagnostic uses, such as what is referred to as point of care diagnostics that in some cases may not take place in a clinical laboratory environment where access to laboratory equipment to effectively enable a spike-in method may be limited.

In some of the embodiments described herein, aqueous droplets are generated from a sample such that each droplet contains one or fewer RNA molecules of interest on average, and reagents necessary for cDNA synthesis and/or amplification (e.g. some embodiments of non- sequencing quantification assays using the combined cDNA synthesis with digital PCR amplification and counting may be referred to as RT-dPCR). The RNA in the droplets is subjected to a cDNA synthesis step to produce a single cDNA strand that is a copy of the RNA. In some embodiments, synthesis of a second cDNA strand may also be performed however it may not be necessary in all embodiments. It will be appreciated by those of ordinary skill that, as described above, the efficiency of the conversion of RNA to cDNA can be very important to the accuracy of the results where the synthesis of cDNA is super-efficient in the volume of the droplet environment.

In some embodiments target specific primer species and/or random hexamers constructed to amplify small RNA are employed in the RT-dPCR process. Examples of primer species enabled to covert small RNA to cDNA include what are referred to as stem-loop RT primers (also referred to as “hairpin-loop” primers, available from the Life Technologies division of Thermo Fisher Scientific). An illustrative example of a stem-loop RT primer is provided in FIG. 3. An additional example of stem-loop primers for generating cDNA is described in Chen, C. F. et al., Nucleic Acids Res. 33 (2005) e179 (which is hereby incorporated by reference herein in its entirety for all purposes). Those of ordinary skill in the art will appreciate that other reagents and designs can be used to initiate reverse transcription of small RNA to generate first- strand cDNA, and therefore the use of stem-loop RT primers should not be considered limiting.

In some embodiments, the stem loop primers may include a barcode, such as a short length sequence of known or random composition that may be used as an identifier of each small RNA in a droplet that may be useful to later identify if experimentally introduced error is present. For example, a random barcode may be incorporated into a cDNA synthesized from a small RNA molecule, where one or more base insertion/deletion events (often referred to as “indels”) may have occurred via polymerase error during subsequent amplification of the cDNA. The barcode may be applied to group the detected amplicons (e.g. via sequencing) together and identify the frequency that a variation occurs, where a variation that occurs at a low rate (e.g. ˜10% or less) may be attributable to experimental error. Barcoding methods may be used for sequencing ‘error correction’.

In some instances, the droplets containing the isolated RNA may already include one or more barcodes that are incorporated into the cDNA during reverse transcription, or hybridize to amplicons produced in the droplets. The barcodes may be used in lieu of fluorescent probes, to detect the presence of a target sequence, or the barcodes can be used in addition to fluorescent probes, to track a multitude of sample sources. A detectable barcode-type label can be any barcode-type label known in the art including, for example, barcoded magnetic beads (e.g., from Applied Biocode, Inc., Santa Fe Springs, Calif.), and nucleic acid sequences. Nucleic acid barcode sequences typically include a set of oligonucleotides ranging from about 4 to about 20 oligonucleotide bases (e.g., 8-10 oligonucleotide bases) and uniquely encode a discrete library member without containing significant homology to any sequence in the targeted sample.

The barcode sequence generally includes features useful in sequencing reactions. For example, the barcode sequences are designed to have minimal or no homopolymer regions, i.e., 2 or more of the same base in a row such as AA or CCC, within the barcode sequence. The barcode sequences are also designed so that they are at least one edit distance away from the base addition order when performing base-by-base sequencing, ensuring that the first and last base do not match the expected bases of the sequence. In certain embodiments, the barcode sequences are designed to be correlated to a particular subject, allowing subject samples to be distinguished. Designing barcodes is shown U.S. Pat. No. 6,235,475, the contents of which are incorporated by reference herein in their entirety.

In some instances, the primers used in the invention (including, e.g., primers having targeting arms flanked with a bridge section) may include barcodes such that the barcodes will be incorporated into the amplified products. For example, the unique barcode sequence could be incorporated into the 5′ end of the primer, or the barcode sequence could be incorporated into the 3′ end of the primer. In some embodiments, the barcodes may be incorporated into the amplified products after amplification. For example, a suitable restriction enzyme (or other endonuclease) may be introduced to a sample, e.g., a droplet, where it will cut off an end of an amplification product so that a barcode can be added with a ligase.

Attaching barcode sequences to nucleic acids is shown in U.S. Pub. 2008/0081330 and PCT/US09/64001, the content of each of which is incorporated by reference herein in its entirety. Methods for designing sets of barcode sequences and other methods for attaching barcode sequences are shown in U.S. Pat. Nos. 6,138,077; 6,352,828; 5,636,400; 6,172,214; 6235,475; 7,393,665; 7,544,473; 5,846,719; 5,695,934; 5,604,097; 6,150,516; RE39,793; U.S. Pat. Nos. 7,537,897; 6172,218; and 5,863,722, the content of each of which is incorporated by reference herein in its entirety.

Some of the embodiments described herein also allow for multiple species of RNA to be detected and digitally counted simultaneously (e.g. multiplexing). For example, numerous one-step reactions may be carried out in parallel in many droplets with primers targeting multiple species of RNA molecule in each droplet. For example, droplets are produced such that each droplet contains either a single RNA target of interest or no targets of interest, as well as multiple species of primer each in sufficient quantity to recognize and produce a cDNA copy of one of the RNA target of interest. In other words, each droplet comprises multiplexed primer species each targeting a specific RNA target in order to detect a plurality of RNA targets from a biological sample in multiple droplets in order to detect a plurality of targets. The individual counts from the detected targets or ratios of individual counts may be used.

As discussed herein, digital PCR is ideal for detection and quantification of small RNA targets. The sensitivity of digital PCR is limited only by the number of independent amplifications that can be analyzed. For example, by combining one-step methodologies the embodiments of the invention enable highly accurate detection with low background noise. In essence, embodiments of the invention increase the accuracy, sensitivity, and selectivity of small RNA detection by counting each RNA molecule after conversion to cDNA, in a single compartment and without any transfer steps that can introduce contamination, loss, or user error. Continuing with the present example, to increase the accuracy of quantitation a reference such as an endogenous or exogenous nucleic acid can be used. For instance, an exogenous nucleic acid can be spiked into the sample in a known concentration and analyzed simultaneously with the small RNA molecules, or and endogenous species, such as mRNA, can be counted simultaneously with one or more small RNA species. The endogenous and exogenous references provide useful normalizing comparators for the target small RNA in the sample.

Also as described above, some embodiments of the invention provide systems and methods for quantifying species of viral RNA. In particular an embodiment is described herein for quantification of retroviral RNA transcribed from reservoirs of latent virus, such as RNA from HIV.

In the embodiments described herein detection of RNA transcribed from latent virus and/or proviruses represent a particularly powerful option when compared to the current methods. In particular embodiments, the methods can be used to determine latent HIV viral load. With respect to HIV, the current “gold standard” VOA assay detects cells that can, when activated, release viruses capable of robust replication (i.e., are replication-competent), and provides an estimate of the frequency of latently infected cells that that must be eliminated to ensure eradication of the HIV infection. However, the VOA assay is expensive, time, and labor intensive, and requires large amounts of blood (120-180 ml) from the HIV positive donor. It has also been shown that the VOA assay tends to under-represent the true in vivo frequency of the replication-competent latent viral reservoir where the extent of the under-estimate may be up to 50-fold. In contrast, assays which quantify specific viral nucleic acids, e.g., in plasma, have been shown to overestimate the amount of replication-competent virus. This overestimate may be the result of detecting non-integrated or degraded viral nucleic acids.

Embodiments of a VOA assay are typically performed on highly purified resting CD4+ T cells (e.g. cells containing latent HIV provirus), which do not produce virus without extra stimulation. In embodiments of the VOA assay, resting CD4+ T cells purified from a peripheral blood sample extracted from an HIV positive donor are stimulated with mitogen phytohemagglutinin (PHA) or with anti-CD3 plus anti-CD28 antibodies in the presence of irradiated peripheral blood mononuclear cells (PBMC) from and HIV negative donor. These stimuli induce global T cell activation, which reverses latency of at least a fraction of cells carrying integrated HIV DNA, which subsequently is transcribed into RNA. The cells also translate necessary enzymes and proteins for packing the viruses into infective virion particles. The virion particles are released from these cells into the supernatant. In some embodiments, the virion particles are incubated with PBMC cells from HIV negative donors or with PBMC cells that have been irradiated to deactivate viruses. The virion particles can then be analyzed after 2-3 weeks with an ELISA assay for HIV p24 antigen in the supernatant, or by analyzing the ‘naïve’ cells incubated with the test cells. As mentioned previously, this VOA method is expensive and inefficient because of the large volume of blood required, long timeline for test completion, and significant manpower required for each analysis. Embodiments of the presently described invention eliminate many of the weaknesses of the VOA assay and provide an efficient means for quantifying the amount of latent virus in HIV positive donors. For example, in some embodiments the purified resting CD4+ T cells are stimulated as described for the VOA assay, however there is no need to culture the stimulated cells with the irradiated PBMC cells in order to amplify the latent virus. Instead, the supernatant is collected after sufficient time to allow for release of the virion particles , and the virion particles concentrated (e.g. via centrifugation and collection of the pellet) and/or purified (e.g. using methods known to those of ordinary skill such as polyethylene glycol (PEG) precipitation, or filtration), followed by direct quantification without further incubation. (It will, however, be appreciated that the stimulated CD4+ T cells can be cultured with irradiated PBMC cells for a period in order to increase the number of virion particles in the supernatant which may increase the sensitivity of the droplet based assay described herein.)

In the presently described example, the concentrated/purified virion particles may be introduced into an emulsion of aqueous droplets so that individual droplets typically contain no more than a single virion particle. The virion particles are subsequently lysed within the droplets and super-efficient reverse transcription of the RNA performed to produce a cDNA product as described elsewhere in the description. The cDNA may represent the entire RNA sequence. In some embodiments it may also be desirable to amplify the cDNA within the droplet to produce substantially identical DNA copies although it will be appreciated that the cDNA may be released from the droplet for amplification. In other embodiments, the cDNA can be directly sequenced, wherein an identifying label, e.g., a barcode, is used to facilitate identifying the original RNA molecules. The super-efficient reverse transcription and/or amplification may be performed using primers targeting the HIV gag region and/or HIV long terminal repeat region (also referred to as LTR), although it will be appreciated that other target regions may be employed. In some instances, the entire cDNA sequence will be determined in order to identify whether the RNA is replication-competent.

In an alternative embodiment the HIV virions may be lysed together as a pool or partitioned into different wells and lysed. The subsequent lysate may be processed further or put directly into the aqueous droplets for super-efficient reverse transcription. Once the sample has been partitioned the RNA or the enzymes or both can be quantified in order to determine a latent viral load. In some embodiments it may be advantageous to incorporate one or more molecular barcodes into the cDNA product produced from the super-efficient reverse transcription. For example, it may be highly desirable to associate a specific barcode to each virion particle in that can be used to identify sequence characteristics specific to each virion. One method for associating a unique barcode to each virion is to use a “merge” step where a droplet is merged with another droplet or stream of aqueous fluid. For instance, the formed droplets may contain primers with a barcode that is unique from other droplets and merged with a stream of aqueous fluid comprising the virion particles. The result of the merge is a droplet with the primer/barcode combined with a virion particle. In other embodiments each droplet may initially include one or more unique (or semi-unique) barcodes that will become incorporated into the cDNA, allowing later identification of the original RNA. It is to be recognized that these same techniques may additionally be used to uniquely identify enzymatic activity by identifying enzymatic products, e.g., nucleic acids produced by the action of individual enzymes that are isolated in a droplet.

In some of the embodiments described herein, it may be desirable to release and sequence the cDNA from the droplets. In some embodiments, the cDNA may be amplified. The sequence composition of the virion particles may be used to identify characteristics that enabled the latent virus to become replication competent as well as targets for drug therapy. Further, the number of replication competent CD4 T cells can be quantified which, as described above, is very important to enable an effective cure of HIV infection. In some embodiments, droplet digital PCR may be used along with or in place of sequencing to identify the replication competent population of latent HIV.

FIG. 11 provides an illustrative example of a workflow for encapsulating barcode labels in droplets with single virions from a sample extracted from a tissue or fluid (e.g. blood). In some embodiments that barcode labels may be incorporated into the droplets at the time of droplet formation, however it may be desirable in some embodiments to merge the barcode labels into the droplets comprising the HIV virions (e.g. droplet-droplet merging or merging droplets with a stream of fluid) that may provide better control of barcode distribution. For example, it may be highly desirable that each droplet has a barcode label comprising sequence composition that has a sufficient degree of uniqueness so that it is easily distinguishable from barcode labels in other droplets. In the present example, each droplet has a single species of barcode label, however in some embodiments more than one species of barcode label may be present in individual droplets so long as the barcode species retain their uniqueness either alone or in combination.

In the example of FIG. 11, the virions are lysed within the droplets and cDNA products produced that incorporate the barcode label into each cDNA product. The cDNA products are subsequently amplified (e.g. in the droplets, or released and amplified outside the droplets such as in a bulk solution), typically to produce clonal populations of substantially identical copies amenable for sequencing, although it will be appreciated that clonal populations are not necessary for all sequencing technologies. The amplified products are sequenced to produce sequence composition of each viral genome identified by the associated barcode sequence. The sequence composition of each viral genome may then be analyzed for a variety of purposes that include, but are not limited to, Viral quantitation, identification of variation associated with resistance to one or more drugs or drug combinations, replication competency, and latent reservoir detection and characterization.

As described above, some embodiments of the invention may alternatively or additively include detection of an enzyme, e.g., a reverse transcriptase or RNAseH, corresponding to the latent viral load. FIG. 9 shows an illustration of the concept and workflow for a digital droplet ELISA assay, one example of an upfront assay that can be coupled to the digital reporter enzyme assay readout. When protein concentrations are too low for standard detection methods (typically low-sub-picomolar), the disclosed methods enables protein quantification by counting individual protein molecules with a fluorescent readout. Droplets containing a single molecule (e.g. in an ELISA sandwich) will be fluorescent, and the number of fluorescent droplets in a population of total droplets will yield a digital count of molecules per volume (e.g. concentration) down to a limit of detection dependent only on the number of droplets examined.

FIG. 9 shows one example ELISA assay format and should not be considered the only or preferred format (e.g. magnetic beads could be added following antibody binding in solution). The protein-containing sample (proteins shown as diamonds with the rare target protein to be counted shown as solid diamonds) is combined with the binding reagents and incubated for a sufficient time to bind into productive complexes.

In the “ELISA Sandwich Formation” step, each target protein molecule is bound to two affinity reagents (each binding separate epitopes of the same target molecule), generating an immunoaffinity “sandwich” complex. In the example shown, one of the affinity reagents (e.g. antibody) is immobilized onto a magnetic bead while the other biotinylated antibody is free in solution. In certain embodiments, the number of magnetic beads (with immobilized antibody) is significantly greater than the number of target proteins in solution, so that single target proteins are bound by single beads. If the second antibody is used at the same time, its concentration should be greater than the number of target molecules, but less than the number of immobilized antibodies. Alternatively, the second antibody can be added following the first binding step (ensuring that all target molecules are bound to the immobilized antibody first).

After the target proteins are bound into sandwich complexes, the magnetic beads are retained by a magnetic field to allow removal of unbound non-target proteins and free antibodies, and washed to remove non-specific binders. Addition of the reporter enzyme (e.g. streptavidin- beta galactosidase) results in binding to the second biotinylated antibody and assembly of the final ELISA sandwich, which is again washed to remove unbound reporter enzyme. The final material (see, e.g., FIG. 10A) is re-suspended in a small volume, along with a fluorogenic substrate, for processing in the digital droplet readout.

FIGS. 10A-10D show a number of different readout ‘modes’ for running the digital droplet readout, following the ELISA sandwich complex construction. In FIG. 10A, more than one magnetic bead is in each droplet, but only a single ELISA sandwich is in any single droplet (e.g. in this case sub-micron magnetic beads are used).

FIG. 10B shows a mode where at most a single bead is in each droplet, with at most one ELISA sandwich.

FIG. 10C shows a mode where the second antibody complexed to the reporter enzyme has been eluted off of the magnetic bead, and the droplets are loaded such that at most one antibody-reporter complex is present in any droplet.

In FIG. 10D, the reporter enzyme itself is released off of the magnetic bead, with droplets loaded such that at most one enzyme molecule is present in any droplet.

Any suitable method can be used for releasing the enzyme from the ELISA sandwich. Exemplary methods include: 1) competition of a desthiobiotin-streptavidin interaction using biotin; 2) reduction of a linker that contains a disulfide bond; 3) enzymatic cleavage of a linker group. Other variations can be considered, and Poisson and non-Poisson models can be used to enable high occupancy loading while still providing quantitative counting. Thus, it is possible to quantify an amount of latent viral load by characterizing an amount of enzyme that is present as a result of latent viral infection.

The methods for evaluating enzymatic activity are not limited to ELISA-type detection, as described above, however. For example, reverse transcriptase activity can be performed by co-encapsulating enzymes resulting from a latent virus with a known substrate (e.g. exogenous RNA) along with a detection assay (e.g. qPCR assay for the exogenous RNA, or the use of a fluorogenic RNA substrate). In droplets having active enzymes and complimentary substrates, new products will be formed that can be detected, e.g., with fluorescent detection or by sequencing the resulting products. Similarly, RNAseH detection would utilize coencapsulation of a substrate (e.g. synthetic RNA/DNA hybrid) together with a detection assay (e.g. qPCR assay for the exogenous DNA that is released from the RNA/DNA hybrid after RNAseH activity or the use of a fluorogenic RNA/DNA substrate). Again, the enzymatic products can be detected and quantified with a variety of techniques, including sequencing and fluorescent detection.

EXAMPLES

FIGS. 4-8 provide examples of data obtained from experiments conducted to detect and quantify small RNA in droplets.

FIGS. 4 and 5 illustrate droplet counts plotted on VIC/FAM scatter or cluster plots from an assay involving miR-16 and Xeno synthetic RNA. As shown in FIG. 4, results of digital PCR duplex assays for quantifying miR-16 and an exogeneous spiked in RNA species are displayed (VIC intensity is shown on the y axis and FAM intensity on the x-axis). At the end of the RT-PCR of a plurality of droplets containing miR-16 and exogenous RNA, the fluorescence emission from each droplet was determined and plotted on a scatter (or cluster) plot based on its wavelength and intensity. Three elliptical circles or gates are shown (many other gating methods can be used) outlining either the cluster of droplets containing species of miR-16, the Xeno RNA spike-in molecules, or droplets containing no target molecules (Neg). All plots shown in FIG. 4 are from the same experiment, with all samples having the same ‘duplex’ assay mixtures containing primers and probe species for detection of Xeno molecules using VIC hydrolysis probes and miR-16 FAM hydrolysis probes, with the different samples A-H having different amounts of either the miR-16 RT primer or input nucleic acid. Sample A shows the results of a positive control dPCR assay using miR-16 cDNA input together with synthetic Xeno RNA, illustrating that the miR16 assay reagents work together with Xeno RT-PCR assay reagents. Sample B shows the results of the duplexed assay with no miR-16 target input and Xeno RNA input, with no background seen for the miR-16 cluster location, illustrating that the digital droplet environment does not result in ‘background’ signal from the RT primer self-priming in the absence of its target (in the gated region of the graph where miR-16 is detected in the positive control, no significant background signal is seen). Sample D show the results with both Xeno and miR-16 synthetic RNA inputs and no miR-16 RT primer added, showing the specificity of the Xeno assay. In Samples E-H the same duplex assay is used with miR-16 RT primer added together with a constant amount of Xeno synthetic RNA and a variable amount of total human RNA (commercial source from a mixture of organs). The RT-dPCR (digital RT-PCR) assay count the same number of Xeno molecule-containing droplets and a variable amount of miR-16 that linearly correlates with the amount of input total RNA added to the sample. Similar to the control sample D compared to Sample C, when the RT primer for miR-16 is omitted from the assay in Sample H there was no background signal detected where miR-16 would be present on the graph (compare Sample H and Sample G).

Additionally, FIG. 6 shows duplex assays quantifying the amount of either miR-16, miR-21, or miR-92a, as well as Xeno RNA spiked in for miR-16 or miR-21 cases (assays listed at the top of each sample, with input RNA listed below each sample). Sample B shows the specificity of the reaction (i.e. no miR-21 is detected when only miR-16 is inputted into the assay). Comparing Samples D, E, and F, no significant signal is detected within the gates for miR-21 and miR-16 when the associated RT primers are omitted from the assay, again illustrating a significant lack of background signal for these species. Samples D and E show the specificity of the reaction for either miR-21 or miR-92a, displaying little background when either specific RT primer is omitted from the reaction, when the input RNAs are the same.

FIG. 7 shows an example of expected results of a triplex RT-dPCR reaction, with Sample A showing the results with both miR-21 and miR-15 RT primers, Sample B showing specific detection of only miR-21 when no miR-16 RT primer is added, and Sample C showing specific detection of only miR-16 when no miR-21RT primer is added. All three samples show the same amount of Xeno synthetic RNA spiked-in, with the Xeno qPCR utilizing both a VIC-probe and and FAM-probe to the same Xeno sequence (thus droplets with a molecule of Xeno RNA hydrolyze both VIC and FAM probes, resulting in these droplets appearing ‘off-axis’ in the scatter plot).

FIG. 8 shows the results of a duplex assay for an endogenous mRNA (POL2RA, on the VIC-axis) and miR-21 (on the FAM-axis), with Sample B showing the lack of detection of miR-21 when miR-21 RT primer is omitted from the assay.

Having described various embodiments and implementations, it should be apparent to those skilled in the relevant art that the foregoing is illustrative only and not limiting, having been presented by way of example only. Many other schemes for distributing functions among the various functional elements of the illustrated embodiments are possible. The functions of any element may be carried out in various ways in alternative embodiments.

Incorporation by Reference

References and citations to other documents, such as patents, patent applications, patent publications, journals, books, papers, web contents, have been made throughout this disclosure. All such documents are hereby incorporated herein by reference in their entirety for all purposes.

Equivalents

The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting on the invention described herein. 

What is claimed is:
 1. A method for detection of latent retrovirus, comprising the steps of: isolating a virion particle in an aqueous droplet surrounded by an immiscible fluid; lysing the virion particle in the aqueous droplet to release an RNA molecule; exposing the RNA molecule to at least one primer capable of hybridizing to at least a portion of the RNA molecule; synthesizing a cDNA product from the RNA molecule; and detecting the cDNA product.
 2. The method of claim 1, wherein detecting comprises amplifying the cDNA product to produce a plurality of substantially identical copies of the cDNA product.
 3. The method of claim 2, further comprising sequencing the substantially identical copies of the cDNA product to produce sequence reads.
 4. The method of claim 2, wherein the copies of cDNA product are detected with fluorescence detection.
 5. The method of claim 1, wherein said detecting step comprises quantifying said cDNA.
 6. The method of claim 1, further comprising introducing an amount of exogenous synthetic RNA, DNA, or mRNA.
 7. The method of claim 6, further comprising normalizing the detected cDNA against the exogenous synthetic RNA, DNA, or mRNA.
 8. The method of claim 1, further comprising collecting the virion particle from an isolated biological sample.
 9. The method of claim 8, wherein the isolated biological sample is a T-cell.
 10. The method of claim 9, wherein the T-cell is a CD4+ T cell.
 11. The method of claim 1, wherein the latent retrovirus a human immunodefficiency virus (HIV).
 12. A method for detecting a latent retrovirus species, the method comprising the steps of: isolating virion RNA in an aqueous droplet surrounded by an immiscible fluid, exposing the virion RNA in the droplet to at least one primer capable of hybridizing to at least a portion of the virion RNA; synthesizing a cDNA product from the virion RNA; and detecting the cDNA product.
 13. The method of claim 12, wherein detecting comprises amplifying the cDNA product to produce a plurality of substantially identical copies of the cDNA product.
 14. The method of claim 13, further comprising sequencing the substantially identical copies of the cDNA product to produce sequence reads.
 15. The method of claim 13, wherein the copies of cDNA product are detected with fluorescence detection.
 16. The method of claim 12, wherein said detecting step comprises quantifying said cDNA.
 17. The method of claim 12, further comprising introducing an amount of exogenous synthetic RNA, DNA, or mRNA.
 18. The method of claim 17, further comprising normalizing the detected cDNA against the exogenous synthetic RNA, DNA, or mRNA.
 19. The method of claim 12, further comprising collecting the virion particle from an isolated biological sample.
 20. The method of claim 19, wherein the isolated biological sample is a T-cell.
 21. The method of claim 20, wherein the T-cell is a CD4+ T cell.
 22. The method of claim 21, wherein the latent retrovirus a human immunodefficiency virus (HIV).
 23. A method for quantifying enzymes corresponding to a latent retrovirus, comprising the steps of: isolating a reverse transcriptase or an RNAseH in an aqueous droplet surrounded by an immiscible fluid, contacting the reverse transcriptase or RNAseH with a molecule that specifically binds to the reverse transcriptase or RNAseH, thereby creating a signal; and detecting the signal.
 24. The method of claim 23, further comprising quantifying the signal.
 25. The method of claim 23, wherein the presence of the reverse transcriptase or the RNAseH is indicative of a latent HIV load.
 26. A method for quantifying enzymes corresponding to a latent retrovirus, comprising the steps of: isolating a reverse transcriptase or an RNAseH in an aqueous droplet surrounded by an immiscible fluid, contacting the reverse transcriptase or RNAseH with a molecule that specifically binds to the reverse transcriptase or RNAseH, thereby quenching a signal, monitoring a plurality of droplets, including the aqueous droplet, for the presence or absence of the signal; and quantifying an amount of enzyme in the droplets.
 27. The method of claim 26, wherein the absence of the signal is indicative of a latent HIV load.
 28. A method for quantifying latent retrovirus, comprising the steps of: isolating a virion particle in an aqueous droplet surrounded by an immiscible fluid; lysing the virion particle in the aqueous droplet to release an RNA molecule; exposing the RNA molecule to at least one primer capable of hybridizing to at least a portion of the RNA molecule; synthesizing a cDNA product from the RNA molecule; and sequencing the cDNA product.
 29. A method for quantifying enzymatic activity corresponding to a latent retrovirus, comprising the steps of: isolating a reverse transcriptase or an RNAseH in an aqueous droplet surrounded by an immiscible fluid, wherein the aqueous droplet comprises a substrate for the reverse transcriptase or an RNAseH, quantifying an amount of product produced by the reverse transcriptase or an RNAseH.
 30. The method of claim 29, wherein quantifying comprises detecting a nucleic acid product.
 31. The method of claim 29, wherein quantifying comprises sequencing a nucleic acid product.
 32. A method for detecting the stage of a disease in a subject, the method comprising: forming fluid partitions comprising virion RNA; exposing the virion RNA in the fluid partitions to at least one primer capable of hybridizing to at least a portion of the virion RNA; synthesizing cDNA products from the virion RNA; determining a distribution of the cDNA products; comparing the determined distribution to an expected distribution of said cDNA products for a stage of a disease; and determining the stage of the disease.
 33. A method for detection of small RNA, the method comprising the steps of: isolating small RNA in an aqueous droplet surrounded by an immiscible fluid, exposing the small RNA in the droplet to at least one primer capable of hybridizing to at least a portion of said small RNA; synthesizing a cDNA product from the small RNA; and detecting the cDNA product.
 34. The method of claim 33, further comprising the step of amplifying the cDNA product to produce a plurality of substantially identical copies of the cDNA product, wherein the substantially identical copies of the cDNA product are detected.
 35. The method of claim 33, wherein said detecting step comprises quantifying said cDNA.
 36. The method of claim 33, wherein said at least one primer comprises a stem-loop primer.
 37. The method of claim 34, wherein said amplifying step comprises quantitative polymerase chain reaction.
 38. The method of claim 33, further comprising introducing an amount of exogenous synthetic RNA, DNA, or mRNA.
 39. The method of claim 38, further comprising normalizing the detected cDNA against the exogenous synthetic RNA, DNA, or mRNA.
 40. The method of claim 34, further comprising sequencing the substantially identical copies of the cDNA products to produce sequence reads.
 41. A method for detecting a plurality of small RNA species, the method comprising the steps of: isolating small RNA in an aqueous droplet surrounded by an immiscible fluid, exposing the small RNA in the droplet to at least one primer capable of hybridizing to at least a portion of the small RNA; synthesizing a cDNA product from the small RNA; and amplifying the cDNA product in said droplet; and detecting said amplified cDNA products. 